Relevant bibliographies by topics / Plasmodium parasite

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Plasmodium parasite'

Author: Grafiati
Published: 4 June 2021
Last updated: 10 February 2022

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Journal articles on the topic "Plasmodium parasite"

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Gutiérrez-López, Rafael, Josué Martínez-de la Puente, Laura Gangoso, Ramón Soriguer, and Jordi Figuerola. "Plasmodium transmission differs between mosquito species and parasite lineages." Parasitology 147, no. 4 (2020): 441–47. http://dx.doi.org/10.1017/s0031182020000062.

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AbstractFactors such as the particular combination of parasite–mosquito species, their co-evolutionary history and the host's parasite load greatly affect parasite transmission. However, the importance of these factors in the epidemiology of mosquito-borne parasites, such as avian malaria parasites, is largely unknown. Here, we assessed the competence of two mosquito species [Culex pipiens and Aedes (Ochlerotatus) caspius], for the transmission of four avian Plasmodium lineages (Plasmodium relictum SGS1 and GRW11 and Plasmodium cathemerium-related lineages COLL1 and PADOM01) naturally infectin
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HANADA, Kentaro, Toshihide MITAMURA, Masayoshi FUKASAWA, Pamela A. MAGISTRADO, Toshihiro HORII, and Masahiro NISHIJIMA. "Neutral sphingomyelinase activity dependent on Mg2+ and anionic phospholipids in the intraerythrocytic malaria parasite Plasmodium falciparum." Biochemical Journal 346, no. 3 (2000): 671–77. http://dx.doi.org/10.1042/bj3460671.

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Sphingolipid metabolism and metabolites are important in various cellular events in eukaryotes. However, little is known about their function in plasmodial parasites. Here we demonstrate that neutral sphingomyelinase (SMase) involved in the sphingomyelin (SM) catabolism is retained by the intraerythrocytic parasite Plasmodium falciparum. When assayed in a neutral pH buffer supplemented with Mg2+ and phosphatidylserine, an activity for the release of the phosphocholine group from SM was detected in parasite-infected, but not in uninfected, erythrocyte ghosts. The SMase activity in the parasite-
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Tewari, Rita, Solabomi A. Ogun, Ruwani S. Gunaratne, Andrea Crisanti, and Anthony A. Holder. "Disruption of Plasmodium berghei merozoite surface protein 7 gene modulates parasite growth in vivo." Blood 105, no. 1 (2005): 394–96. http://dx.doi.org/10.1182/blood-2004-06-2106.

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Abstract Merozoite invasion of red blood cells is crucial to the development of the parasite that causes malaria. Merozoite surface proteins (MSPs) mediate the first interaction between parasite and erythrocyte. In Plasmodium falciparum, they include a complex of products from at least 3 genes (msp1, msp6, and msp7), one of which, msp7, is part of a gene family containing 3 and 6 adjacent members in Plasmodium yoelii and Plasmodium falciparum, respectively. We have identified and disrupted msp7 in the Plasmodium berghei gene family. The protein is expressed in schizonts and colocalizes with MS
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Antinori, Spinello, Laura Galimberti, Laura Milazzo, and Mario Corbellino. "BIOLOGY OF HUMAN MALARIA PLASMODIA INCLUDING PLASMODIUM KNOWLESI." Mediterranean Journal of Hematology and Infectious Diseases 4, no. 1 (2012): e2012013. http://dx.doi.org/10.4084/mjhid.2012.013.

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Malaria is a vector-borne infection caused by unicellular parasite of the genus Plasmodium. Plasmodia are obligate intracellular parasites that in humans after a clinically silent replication phase in the liver are able to infect and replicate within the erythrocytes. Four species (P.falciparum, P.malariae, P.ovale and P.vivax) are traditionally recognized as responsible of natural infection in human beings but the recent upsurge of P.knowlesi malaria in South-East Asia has led clinicians to consider it as the fifth human malaria parasite. Recent studies in wild-living apes in Africa have reve
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Wulandari, Diah Anggraini, and Muhammad Safaat. "REVIEW: PERAN NANOPARTIKEL DALAM MENGHAMBAT PERTUMBUHAN PARASIT Plasmodium PENYEBAB MALARIA." Jurnal Bioteknologi & Biosains Indonesia (JBBI) 8, no. 1 (2021): 124–36. http://dx.doi.org/10.29122/jbbi.v8i1.4503.

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Review: The Role of Nanoparticles in Inhibiting the Growth of the Plasmodium Parasite Causing Malarial Disease Malaria is a health problem in Indonesia with the most cases in eastern parts of Indonesia. This study provides an overview of the potential of nanoparticles in inhibiting malaria vectors and the growth of Plasmodium parasites that causes malaria based on the latest literature as reference materials and future research ideas. Nanoparticle can be synthesized using three methods i.e. physical, chemical and biological synthesis. The use of nanoparticles with biological method is highly r
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Smith, Lauren M., Francis C. Motta, Garima Chopra, et al. "An intrinsic oscillator drives the blood stage cycle of the malaria parasite Plasmodium falciparum." Science 368, no. 6492 (2020): 754–59. http://dx.doi.org/10.1126/science.aba4357.

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The blood stage of the infection of the malaria parasite Plasmodium falciparum exhibits a 48-hour developmental cycle that culminates in the synchronous release of parasites from red blood cells, which triggers 48-hour fever cycles in the host. This cycle could be driven extrinsically by host circadian processes or by a parasite-intrinsic oscillator. To distinguish between these hypotheses, we examine the P. falciparum cycle in an in vitro culture system and show that the parasite has molecular signatures associated with circadian and cell cycle oscillators. Each of the four strains examined h
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Galinski, Mary R. "Functional genomics of simian malaria parasites and host–parasite interactions." Briefings in Functional Genomics 18, no. 5 (2019): 270–80. http://dx.doi.org/10.1093/bfgp/elz013.

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AbstractTwo simian malaria parasite species, Plasmodium knowlesi and Plasmodium cynomolgi, cause zoonotic infections in Southeast Asia, and they have therefore gained recognition among scientists and public health officials. Notwithstanding, these species and others including Plasmodium coatneyi have served for decades as sources of knowledge on the biology, genetics and evolution of Plasmodium, and the diverse ramifications and outcomes of malaria in their monkey hosts. Experimental analysis of these species can help to fill gaps in knowledge beyond what may be possible studying the human mal
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Collins, William E., and Geoffrey M. Jeffery. "Plasmodium malariae: Parasite and Disease." Clinical Microbiology Reviews 20, no. 4 (2007): 579–92. http://dx.doi.org/10.1128/cmr.00027-07.

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SUMMARY A review of the life history of Plasmodium malariae, the quartan malaria parasite of humans, is presented. Much of the information is based on data obtained from induced infections in humans who were given malaria therapy for the treatment of neurosyphilis between 1940 and 1963. Prepatent periods (i.e., the time until the first day of parasite detection) fever episodes, and maximum parasitemias as a result of infection with P. malariae were obtained and are presented. Experimental and known vectors of the parasite are also discussed. Splenectomized chimpanzees and New World monkeys are
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Amin Siddiq Sumi, Hanung Adi Nugroho, and Rudy Hartanto. "A Systematic Review on Automatic Detection of Plasmodium Parasite." International Journal of Engineering and Technology Innovation 11, no. 2 (2021): 103–21. http://dx.doi.org/10.46604/ijeti.2021.6094.

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Plasmodium parasite is the main cause of malaria which has taken many lives. Some research works have been conducted to detect the Plasmodium parasite automatically. This research aims to identify the development of current research in the area of Plasmodium parasite detection. The research uses a systematic literature review (SLR) approach comprising three stages, namely planning, conducting, and reporting. The search process is based on the keywords which were determined in advance. The selection process involves the inclusion and exclusion criteria. The search yields 45 literatures from fiv
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Simão-Gurge, Raquel M., Neha Thakre, Jessica Strickland, et al. "Activation of Anopheles stephensi Pantothenate Kinase and Coenzyme A Biosynthesis Reduces Infection with Diverse Plasmodium Species in the Mosquito Host." Biomolecules 11, no. 6 (2021): 807. http://dx.doi.org/10.3390/biom11060807.

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Malaria parasites require pantothenate from both human and mosquito hosts to synthesize coenzyme A (CoA). Specifically, mosquito-stage parasites cannot synthesize pantothenate de novo or take up preformed CoA from the mosquito host, making it essential for the parasite to obtain pantothenate from mosquito stores. This makes pantothenate utilization an attractive target for controlling sexual stage malaria parasites in the mosquito. CoA is synthesized from pantothenate in a multi-step pathway initiated by the enzyme pantothenate kinase (PanK). In this work, we manipulated A. stephensi PanK acti
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Dissertations / Theses on the topic "Plasmodium parasite"

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Curra, Chiara. "Protein trafficking and host cell remodeling in malaria parasite infection." Thesis, Montpellier 2, 2010. http://www.theses.fr/2010MON20219.

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Pour assurer ses besoins de croissance, multiplication, et survie, Plasmodium modifie sa cellule hôte, l'érythrocyte, après l'invasion. Le parasite met en place ainsi un système d'échanges (import/export) avec sa cellule hôte et le milieu extérieur. Nous avons identifié dans la base de données de Plasmodium berghei, le parasite de rongeurs, une famille de gènes, sep, correspondant à la famille etramp chez Plasmodium falciparum. Cette famille de gènes code pour des petites protéines exportées, et conservées dans tout le genre Plasmodium. Les protéines SEP (13?16 kDa) contiennent en N-terminal u
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Walker, Alison Dalgity. "Protein variation in the malaria parasite Plasmodium falciparum." Thesis, University of Edinburgh, 1986. http://hdl.handle.net/1842/13171.

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Ranford-Cartwright, Lisa C. "Cross-fertilisation in the malaria parasite Plasmodium falciparum." Thesis, University of Edinburgh, 1992. http://hdl.handle.net/1842/14248.

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The objective of this work has been to investigate the frequency of cross-fertilisation between gametes of genetically distinct clones of the human malaria parasite <i>Plasmodium falciparum</i>. Previous genetic experiments involving both rodent malaria parasites <i>in vivo</i> and human malaria parasites <i>in vitro</i> have demonstrated higher than expected numbers of recombinants among the progeny of crosses. It has been suggested that this could be due to a favouring of cross-fertilisation over self-fertilisation in the mosquito phase of the life-cycle. The work has involved examining the
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Green, Judith Louise. "Genes encoding rhoptry proteins of the malaria parasite plasmodium." Thesis, University College London (University of London), 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.300303.

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Chadwick, Catherine Joyce. "Immunocytochemical studies on the rodent malaria parasite Plasmodium chabaudi." Thesis, University of Liverpool, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.357377.

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Wall, Bridget (Bridget Anne). "Engineered tools for studying the malaria parasite plasmodium falciparum." Thesis, Massachusetts Institute of Technology, 2015. http://hdl.handle.net/1721.1/98923.

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Thesis: Ph. D., Massachusetts Institute of Technology, Department of Biological Engineering, 2015.<br>This electronic version was submitted by the student author. The certified thesis is available in the Institute Archives and Special Collections.<br>Cataloged from PDF student-submitted version of thesis.<br>Includes bibliographical references (pages 120-136).<br>New techniques to both prevent and treat the disease malaria are necessary. To develop these novel strategies, innovative tools must be designed to study the basic biology within Plasmodium falciparum and characteristics of the patho
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Sharkey, Andrew M. "Genetic variation in the rodent malaria parasite Plasmodium chabaudi." Thesis, University of Edinburgh, 1989. http://hdl.handle.net/1842/14391.

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Bucsu, Eva. "Plasmodium chabaudi adami : vaccine antigens and antigenic variation /." Connect to thesis, 2003. http://repository.unimelb.edu.au/10187/2881.

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There is an abundance of information available on the molecular mechanisms of antigenic variation in Plasmodium falciparum. The variant antigen PfEMP1, which mediates antigenic variation as well as cytoadherence and rosetting, has been extensively characterised. Genes coding for the antigen belong to the gene family var, and several var genes have been cloned and characterised. The rodent malaria parasite P. chabaudi is a widely studied in vivo model for P. falciparum. The P. c. chabaudi AS parasite strain has been shown to exhibit antigenic variation and the variant antigen has been detected
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De, Aguiar J. C. S. "Studies on the polymorphic schizont antigen of Plasmodium chabaudi." Thesis, Open University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.383640.

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Aidoo, Michael. "Cytotoxic T lymphocytes and Plasmodium falciparum malaria." Thesis, Open University, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.309865.

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Books on the topic "Plasmodium parasite"

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author, Blake John G., Loiselle Bette A. author, Penrose Amanda S. author, Parker Patricia G. author, and Ricklefs Robert E. author, eds. Diversity, prevalence, and host specificity of avian Plasmodium and Haemoproteus in a Western Amazon assemblage. American Ornithologists' Union, 2013.

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Iqbal, M. P. Investigation of the TFIIB and fibrillarin genes in the human malaria parasite plasmodium falciparum. UMIST, 1996.

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1941-, Eaton John Wallace, Meshnick Steven R, and Brewer George J. 1930-, eds. Malaria and the red cell 2: Proceedings of the Second Workshop on Malaria and the Red Cell, held in Ann Arbor, Michigan, October 24, 1988. A.R. Liss, 1989.

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World Health Organization (WHO). Malaria rapid diagnostic test performance: Results of WHO product testing of malaria RDTs : round 1 (2008). World Health Organization on behalf of the Special Programme for Research and Training in Tropical Diseases, 2009.

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Garnham, P. C. C. Catalogue of the Garnham Collection of malaria parasites and other haemosporidia. Cambridge University Press London, 1988.

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Garnham, P. C. C. Catalogue of the Garnham Collection of malaria parasites and other haemosporidia. The Wellcome Trust, 1986.

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Garnham, P. C. C. Catalogue of the Garnham collection of malaria parasites and other haemosporidia. Cambridge University Press, 1986.

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Wyborny, Sheila. Parasites! - The Malaria Parasite (Parasites!). KidHaven Press, 2005.

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Mayer, Ghislaine. Plasmodium Falciparum: Morphology, Life Cycle and Health Impact. Nova Science Publishers, Incorporated, 2013.

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Sherman, Irwin W. Malaria: Parasite Biology, Pathogenesis, and Protection. ASM Press, 1998.

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Book chapters on the topic "Plasmodium parasite"

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Lambrechts, Louis, and Jacob C. Koella. "Evolutionary aspects of Anopheles-Plasmodium interactions." In Ecology of parasite-vector interactions. Wageningen Academic Publishers, 2013. http://dx.doi.org/10.3920/978-90-8686-744-8_6.

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Cox-Singh, Janet, Balbir Singh, and Sanjeev Krishna. "Plasmodium knowlesi: the Fifth Human Malarial Parasite." In Emerging Infections 9. ASM Press, 2014. http://dx.doi.org/10.1128/9781555816803.ch13.

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Le Roch, Karine, and Elizabeth Winzeler. "The Transcriptome of the Malaria Parasite Plasmodium falciparum." In Molecular Approaches to Malaria. ASM Press, 2014. http://dx.doi.org/10.1128/9781555817558.ch5.

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Newbold, C. I. "Parasite Antigens in Protection, Diagnosis and Escape: Plasmodium." In Current Topics in Microbiology and Immunology. Springer Berlin Heidelberg, 1985. http://dx.doi.org/10.1007/978-3-662-09197-5_5.

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Kilejian, A., Y. D. Sharma, and Y. F. Yang. "The Knob Protein Gene of Plasmodium Falciparum." In Host-Parasite Cellular and Molecular Interactions in Protozoal Infections. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72840-2_35.

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Hirai, Makoto. "Fertilization Mechanisms of the Rodent Malarial Parasite Plasmodium berghei." In Sexual Reproduction in Animals and Plants. Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54589-7_27.

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Berry, Colin, John B. Dame, Ben M. Dunn, and John Kay. "Aspartic Proteinases from the Human Malaria Parasite Plasmodium Falciparum." In Aspartic Proteinases. Springer US, 1995. http://dx.doi.org/10.1007/978-1-4615-1871-6_67.

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Tyas, L., R. P. Moon, H. Loetscher, et al. "Plasmepsins I and II from the Malarial Parasite Plasmodium falciparum." In Aspartic Proteinases. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4615-5373-1_57.

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Pichugin, Alexander, and Urszula Krzych. "Detection of Plasmodium berghei and Plasmodium yoelii Liver-Stage Parasite Burden by Quantitative Real-Time PCR." In Malaria Vaccines. Springer New York, 2015. http://dx.doi.org/10.1007/978-1-4939-2815-6_7.

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Heidrich, Hans-G., Werner Strych, Friedrich Lottspeich, and Arja Miettinen-Baumann. "Antigens of Plasmodium Falciparum Merozoites: Identification, Isolation and Functional Characterization." In Host-Parasite Cellular and Molecular Interactions in Protozoal Infections. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/978-3-642-72840-2_30.

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Conference papers on the topic "Plasmodium parasite"

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Abdul-Nasir, Aimi Salihah, Mohd Yusoff Mashor, and Zeehaida Mohamed. "Clustering approach for unsupervised segmentation of malarial Plasmodium vivax parasite." In THE 2ND INTERNATIONAL CONFERENCE ON APPLIED SCIENCE AND TECHNOLOGY 2017 (ICAST’17). Author(s), 2017. http://dx.doi.org/10.1063/1.5005337.

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Yang, Feng, Nicolas Quizon, Hang Yu, et al. "Cascading YOLO: automated malaria parasite detection for Plasmodium vivax in thin blood smears." In Computer-Aided Diagnosis, edited by Horst K. Hahn and Maciej A. Mazurowski. SPIE, 2020. http://dx.doi.org/10.1117/12.2549701.

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Yu, Xinran, Turgay Korkmaz, Timothy G. Lilburn, Hong Cai, Jianying Gu, and Yufeng Wang. "Heavy path mining reveals novel protein-protein associations in the malaria parasite plasmodium falciparum." In 2014 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2014. http://dx.doi.org/10.1109/bibm.2014.6999137.

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Gatc, Jullend, and Febri Maspiyanti. "Plasmodium Parasite Detection on Thin Blood Smear Image using Double Thresholding and BLOB Analysis." In 2018 International Conference on Applied Engineering (ICAE). IEEE, 2018. http://dx.doi.org/10.1109/incae.2018.8579407.

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Nagaram, Nagadevi Bala, Suresh Rasappan, and Naresh Kumar Jothi. "The effect of backstepping control technique to break-up the life cycle of plasmodium parasite." In THE 11TH NATIONAL CONFERENCE ON MATHEMATICAL TECHNIQUES AND APPLICATIONS. AIP Publishing, 2019. http://dx.doi.org/10.1063/1.5112202.

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Gatc, Jullend, Febri Maspiyanti, Devvi Sarwinda, and Aniati Murni Arymurthy. "Plasmodium parasite detection on Red Blood Cell image for the diagnosis of malaria using double thresholding." In 2013 International Conference on Advanced Computer Science and Information Systems (ICACSIS). IEEE, 2013. http://dx.doi.org/10.1109/icacsis.2013.6761605.

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Yu, Xinran, Hao Zhang, Timothy G. Lilburn, et al. "Just-in-time expression of influential genes in the cellular networks of the malaria parasite Plasmodium falciparum during the red blood cycle." In 2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM). IEEE, 2016. http://dx.doi.org/10.1109/bibm.2016.7822526.

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Mubarok, Akhmad, Heny Arwati та Yoes Prijatna Dahlan. "Correlation between Parasite Density with TNF-α and IL-10 in Plasmodium Falciparum Infected Patients in East Sumba District, East Nusa Tenggara Province". У 2nd International Conference Postgraduate School. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0007544004120417.

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Nela, Frieti Vega, Heny Arwati та Yoes Prijatna Dachlan. "Correlation of Parasite Density with Plasma Level of TNF-α and IL-10 in Patients Infected by Plasmodium Vivax in East Sumba District, East Nusa Tenggara Province". У 2nd International Conference Postgraduate School. SCITEPRESS - Science and Technology Publications, 2018. http://dx.doi.org/10.5220/0007542203250328.

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Rocha, Maura G. R., Rodrigo M. S. Veras, Maíla L. Claro, Laurindo S. Britto Neto, and Kelson R. T. Aires. "Análise Comparativa de Versões YOLO na Detecção e Identificação de Parasitas da Malária." In Simpósio Brasileiro de Computação Aplicada à Saúde. Sociedade Brasileira de Computação - SBC, 2021. http://dx.doi.org/10.5753/sbcas.2021.16066.

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A malária é uma doença endêmica causada pelo parasita Plasmodium que pode ser fatal em muitas regiões do mundo. Alguns pesquisadores estão utilizando conceitos de aprendizagem de máquina para detectar e classificar células infectadas pelo parasita Plasmodium. Este trabalho apresenta um estudo comparativo de três versões recentes da rede neural convolucional You Only Look Once (YOLO), são elas a: YOLOv4, Scaled-YOLOv4 e YOLOv5. Foi utilizado a base de dados MP-IDB que possui 210 imagens com o parasita Plasmodium. Os modelos alcançaram excelentes resultados, tendo o melhor resultado com mAP e pre
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Reports on the topic "Plasmodium parasite"

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Piper, Robert C. Parasite Lactate Dehydrogenase for Diagnosis of Plasmodium Falciparum. Phase II. Defense Technical Information Center, 1997. http://dx.doi.org/10.21236/adb230017.

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Prachumsri, Jetsumon. Proteomic Study of Human Malaria Parasite Plasmodium Vivax Liver Stages for Development of Vaccines and Drugs. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada494445.

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